Kowal Brian F, Turco John, Nangia Ajay K
Dartmouth Medical School, Hanover, New Hampshire, USA.
Fertil Steril. 2006 Apr;85(4):1059.e1-4. doi: 10.1016/j.fertnstert.2005.09.056.
To present a case of primary male infertility with severe oligospermia and hyperpigmented skin as the main presenting clinical signs.
Case report.
University-affiliated teaching hospital.
PATIENT(S): A 32-year-old male with severe oligospermia and his 31-year-old female partner with normal cycles.
INTERVENTION(S): Hydrocortisone, fludrocortisone, methimazole, and eventual IVF.
MAIN OUTCOME MEASURE(S): Improved semen analysis, correction of Addison's disease, correction of hyperthyroidism, and ART pregnancy.
RESULT(S): Severe oligospermia of 5 million per milliliter with 15% motility and ACTH level of 2,800 pg/mL on presentation. Endocrinology evaluation revealed cortisol of <0.1 microg/dL, and Cortrosyn test showed no response (Addison's disease). The patient was incidentally found to have a thyroid stimulating hormone level of <0.1 microIU/mL, T4 of 9.5 microg/dL, Free T4 Index calculation of 11.6 microg/dL, and quantitative triiodothyronine of 273 ng/dL on presentation. His Addison's disease was managed with hydrocortisone and fludrocortisone, and his hyperthyroidism, with methimazole. Semen parameters increased to 34 million per milliliter with 45% motility and 5% Kruger morphology 1 year after initial presentation. Hormone parameters normalized. Rather than allowing for more time for natural conception or IUI, the couple decided to proceed with IVF because of insurance coverage before semen parameters normalized.
CONCLUSION(S): This is the first reported case of Addison's disease presenting as male infertility with hyperpigmentation of the skin being the only other presenting sign. The underlying etiology of the Addison's in this case remains uncertain, but it is presumed because of autoimmunity. Addison's disease may be associated with hyperthyroidism, and hyperthyroidism may have contributed to the oligospermia. This case highlights why men with abnormal semen parameters should be thoroughly evaluated before proceeding with assisted reproduction.
报告一例以严重少精子症和皮肤色素沉着为主要临床表现的原发性男性不育病例。
病例报告。
大学附属医院教学医院。
一名32岁严重少精子症男性及其31岁月经周期正常的女性伴侣。
氢化可的松、氟氢可的松、甲巯咪唑,最终进行体外受精。
精液分析改善、艾迪生病纠正、甲状腺功能亢进纠正及辅助生殖技术妊娠。
初诊时精液严重少精子症,每毫升500万,活力15%,促肾上腺皮质激素水平2800 pg/mL。内分泌评估显示皮质醇<0.1 μg/dL,促肾上腺皮质激素释放激素试验无反应(艾迪生病)。患者初诊时意外发现促甲状腺激素水平<0.1 μIU/mL,T4为9.5 μg/dL,游离T4指数计算值为11.6 μg/dL,总三碘甲状腺原氨酸为273 ng/dL。其艾迪生病采用氢化可的松和氟氢可的松治疗,甲状腺功能亢进采用甲巯咪唑治疗。初诊1年后精液参数增至每毫升3400万,活力45%,克鲁格形态学正常率5%。激素参数恢复正常。由于精液参数未恢复正常前有保险覆盖,这对夫妇决定不等待更多自然受孕或宫腔内人工授精时间,而是直接进行体外受精。
这是首例报告的以皮肤色素沉着为唯一其他表现体征的艾迪生病导致男性不育病例。该病例中艾迪生病的潜在病因仍不确定,但推测为自身免疫性。艾迪生病可能与甲状腺功能亢进有关,而甲状腺功能亢进可能导致了少精子症。该病例凸显了为什么精液参数异常的男性在进行辅助生殖之前应进行全面评估。